Evidence map›Paper›PMID 39953336›Full record

ArticleClinical rheumatology2025

Haptoglobin as a novel predictor of visceral involvement and relapse in adult IgAV patients.

Matija Bajželj, Nina Visočnik, Katjuša Mrak Poljšak, Matjaž Hladnik, Katja Lakota, Alojzija Hočevar

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Article in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Matija BajželjDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Nina VisočnikVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic Barcelona, IDIBAPS, Barcelona, Spain.
Katjuša Mrak PoljšakDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Matjaž HladnikFaculty of Mathematics, Natural Sciences and Information Technologies, University of Primorska, Koper, Slovenia.
Katja LakotaDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia. katja.lakota@guest.arnes.si.ORCID http://orcid.org/0000-0002-8062-7908
Alojzija HočevarDepartment of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Funding

Javna Agencija za Raziskovalno Dejavnost RS J7-60132Javna Agencija za Raziskovalno Dejavnost RS P3-0314
6 · The paper itself

Abstract

introductionIgA vasculitis (IgAV) can present as skin-limited or systemic disease, which can be severe in adults. Predictive markers for visceral involvement are suboptimal. Considering haptoglobin's role as an acute phase reactant, we evaluated whether its differential expression in IgAV patients' skin and leukocytes is also reflected systemically in a larger cohort of adult IgAV patients. Additionally, soluble form of haptoglobin scavenger receptor CD163 was measured in IgAV patient serum.

methodsWe re-analyzed RNA sequencing data from leukocytes and skin biopsies of treatment-naïve adult IgAV patients: (1) IgAV nephritis (n = 3), (2) skin-limited IgAV (n = 3), and healthy controls (n = 3). Haptoglobin serum level was measured in 178, and haptoglobin genotyping was performed in 91 treatment-naïve adult IgAV patients. Serum sCD163 was measured in 60 IgAV patients and 22 HC.

resultsTranscriptomic data of leukocytes and skin of IgAV nephritis patients identified haptoglobin as a hub gene, based on protein-protein interaction network. Haptoglobin serum level was elevated in IgAV patients with nephritis or gastrointestinal involvement compared to other IgAV patients. Patients who relapsed during follow-up had decreased haptoglobin serum level at disease presentation compared to non-relapsing patients. Haptoglobin genotyping did not show differences between genotype groups regarding clinical presentation and laboratory parameters. Serum sCD163 was significantly higher in IgAV nephritis patients compared to HC.

conclusionWe identified haptoglobin as a novel marker of visceral involvement and relapse in adult IgAV, while sCD163 is linked to renal involvement. Further studies will confirm the clinical utility of haptoglobin as biomarker in IgAV. Key Points • Haptoglobin expression is upregulated in leukocytes and skin of adult IgAV with renal involvement. • Haptoglobin serum level is elevated in IgAV patients with visceral involvement. • Patients with IgAV relapse have lower haptoglobin at disease presentation.

Indexed as

HaptoglobinsImmunoglobulin AAdultAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenFemaleHumansLeukocytesMaleMiddle AgedReceptors, Cell SurfaceRecurrenceSkinAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenHaptoglobinsImmunoglobulin AReceptors, Cell SurfaceHaptoglobinIgA vasculitisTranscriptomic data

Identifiers

PMID39953336
PMCPMC11993498

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